Zobrazeno 1 - 10
of 176
pro vyhledávání: '"acyl carnitine"'
Autor:
Takehito Okui, Shiori Kuraoka, Masaya Iwashita, Rei Itagawa, Taku Kasai, Masanori Aikawa, Sasha A. Singh, Elena Aikawa
Publikováno v:
Frontiers in Molecular Biosciences, Vol 11 (2024)
Introduction: Carnitine O-octanoyltransferase (CROT) is a well-established peroxisomal enzyme involved in liver fatty acid oxidation, but less is known about its recently discovered role in promoting vascular calcification, and whether CROT-dependent
Externí odkaz:
https://doaj.org/article/59d59852e3244becb85811d9c1542387
Autor:
Julia Krause, Alexander Nickel, Alexandra Madsen, Hamish M. Aitken-Buck, A. M. Stella Stoter, Jessica Schrapers, Francisco Ojeda, Kira Geiger, Melanie Kern, Michael Kohlhaas, Edoardo Bertero, Patrick Hofmockel, Florian Hübner, Ines Assum, Matthias Heinig, Christian Müller, Arne Hansen, Tobias Krause, Deung-Dae Park, Steffen Just, Dylan Aïssi, Daniela Börnigen, Diana Lindner, Nele Friedrich, Khaled Alhussini, Constanze Bening, Renate B. Schnabel, Mahir Karakas, Licia Iacoviello, Veikko Salomaa, Allan Linneberg, Hugh Tunstall-Pedoe, Kari Kuulasmaa, Paulus Kirchhof, Stefan Blankenberg, Torsten Christ, Thomas Eschenhagen, Regis R. Lamberts, Christoph Maack, Justus Stenzig, Tanja Zeller
Publikováno v:
Journal of Translational Medicine, Vol 21, Iss 1, Pp 1-16 (2023)
Abstract Background Long-chain acyl-carnitines (ACs) are potential arrhythmogenic metabolites. Their role in atrial fibrillation (AF) remains incompletely understood. Using a systems medicine approach, we assessed the contribution of C18:1AC to AF by
Externí odkaz:
https://doaj.org/article/8c183ecc7563479ba469a156b176a394
Akademický článek
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Autor:
Chunyan Zhang, Drun Dha, Yuxuan Cheng, Ya Ma, Yan Meng, Drun Tse, Dolma Ngawang, Pedrun Dekyi, Tao Jiang, Yang Shu, Jiayi Cui, Jing Li, Yaping Tian
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: The purpose of the study was to investigate the levels of amino acids and acylcarnitines in newborns of the Tibet Autonomous Region for the first time and to provide an experimental basis for the diagnosis of genetic metabolic diseases.Me
Externí odkaz:
https://doaj.org/article/f3701b4386274994870d63d7606460e2
Autor:
Kaustuv Bhattacharya, Walid Matar, Adviye Ayper Tolun, Beena Devanapalli, Sue Thompson, Troy Dalkeith, Kate Lichkus, Michel Tchan
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background Ketone bodies form a vital energy source for end organs in a variety of physiological circumstances. At different times, the heart, brain and skeletal muscle in particular can use ketones as a primary substrate. Failure to generat
Externí odkaz:
https://doaj.org/article/9561fcfc8ad44394981eb963dea606ec
Publikováno v:
Clinical and Experimental Obstetrics & Gynecology, Vol 49, Iss 5, p 121 (2022)
Background: To evaluate the feasibility of serum microelements, amino acids and acyl carnitine levels to predict maternal complications and adverse infant outcomes in pregnancies complicated by preeclampsia. Methods: We launched a prospective study i
Externí odkaz:
https://doaj.org/article/5d2fc10776b743debb0074e2d5edbb88
Akademický článek
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Publikováno v:
Biomolecules, Vol 11, Iss 4, p 521 (2021)
The SLC25A20 transporter, also known as carnitine acyl-carnitine carrier (CAC), catalyzes the transport of short, medium and long carbon chain acyl-carnitines across the mitochondrial inner membrane in exchange for carnitine. The 30-year story of the
Externí odkaz:
https://doaj.org/article/96af68225e8a4324bc77c6991f8b28fb
Autor:
Vinayasree. C, K, Mohan Naidu., Muralinath. E, Pavan Eswar Reddy. K, Pavan Kumar. K, Guruprasad. M, Sravani Pragna. K
Medium - chain acetyl - CoA dehydrogenase (MCAD) deficiency ia a rare inherited metabolic disorder that shows its influence on the bodys capability to breakdown fatty acids for energy. The symptoms of classical MCAD deficiency typically manifest espe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51d8ec22ba126077ae234112d4bd72dc
Akademický článek
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